Variant report

Variant	rs9690791
Chromosome Location	chr7:127105823-127105824
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs17864930	0.83[YRI][hapmap]
rs17865100	0.87[YRI][hapmap]
rs17865103	0.83[YRI][hapmap]
rs17865208	1.00[AMR][1000 genomes]
rs17866916	0.83[YRI][hapmap];0.80[AFR][1000 genomes]
rs6959473	0.83[YRI][hapmap]
rs73461354	1.00[AMR][1000 genomes]
rs7786739	1.00[AMR][1000 genomes]
rs7798749	0.83[YRI][hapmap]
rs7812278	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1820283	chr7:127101187-127110765	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127097400-127116000	Weak transcription	Pancreas	Pancrea

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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